15073-00-4
15073-00-4
Chemical Structure
4α-Methylcholesterol
- CAS No.: 15073-00-4
- Formula:C28H48O
- Molecular Weight:400.68
IUPAC Name: (3S,4S,8S,9S,10R,13R,14S,17R)-4,10,13-trimethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
InChIKey: PZELUKPNJYWGOY-WKKZOLDUSA-N
SMILES: C[C@@]12[C@]3([H])[C@](CC=C1[C@@H]([C@H](CC2)O)C)([H])[C@@]4([H])[C@](CC3)([C@@](CC4)([H])[C@H](C)CCCC(C)C)C
Biological Activity: 4α-Methylcholesterol is a Cholesterol derivative. 4α-Methylcholesterol can oxidize 3-hydroxy steroid, with the apparent Km of 12.6 μM[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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4α-Methylcholesterol | 99.90% | 4α-Methylcholesterol is a Cholesterol derivative. 4α-Methylcholesterol can oxidize 3-hydroxy steroid, with the apparent Km of 12.6 μM. | ||||||||||||||||||||
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References
- [1]. Smith AG, et, al. Studies of the substrate specificity of cholesterol oxidase from Nocardia erythropolis in the oxidation of 3-hydroxy steroids. Biochem Soc Trans. 1975;3(5):675-7. [Content Brief]
- [2]. Kokke WCMC, et, al. Isolation and synthesis of 23-methyl-22-dehydrocholesterol -a marine sterol of biosynthetic significance. Tetrahedron Letters. 1979; 20(18):3601-3604.
Keywords
